A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449081



Internal ID21106634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34463416..34547376hg38UCSC Ensembl
chr10:34752344..34836304hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3883961
hg1983961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177327
Samples
Known GenesPARD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449081
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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